SLC19A2, solute carrier family 19 member 2, 10560

N. diseases: 70; N. variants: 15
Disease: Venous Thromboembolism ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2038024
rs2038024
Entrez Id: 10560
Gene Symbol: SLC19A2
SLC19A2
CUI: C1861172
Disease:
Venous Thromboembolism 		0.700 GeneticVariation GWASDB A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. 22672568 2012